《Table 1Scientific committees at the EMA.》

《Table 1Scientific committees at the EMA.》   提示：宽带有限、当前游客访问压缩模式
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《欧盟监管环境视角下的传统医药全球化》


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An application must be submitted electronically and in a distinct format，as a Common Technical Document.The content depends on the type of procedure，as described above，and on the type of application:（1）Marketing authorization:full application—for new medicinal products，bibliographic application—for known medicinal products with well-established use，and hybrid forms may be used；（2）Registration:Bibliographic application with additional data on safety if necessary—only for traditional herbal medicinal products.

图表编号XD0061015200    严禁用于非法目的
绘制时间2019.02.01
作者Werner Knoess、Jacqueline Wiesner
绘制单位Federal Institute for Drugs and Medical Devices、Federal Institute for Drugs and Medical Devices
更多格式高清、无水印（增值服务）

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